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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864809Generated: October 30, 2026

2-Methoxyethylamine → N-2-methoxyethyl-1-benzyloxycarbonylpiperidine-4-oxyacetamide

https://huagongshe.com/reaction/864809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
ReactantEthyl 1-benzyloxycarbonylpiperidine-4-oxyacetateHCID 23370004—
ProductN-2-methoxyethyl-1-benzyloxycarbonylpiperidine-4-oxyacetamideHCID 18918307—

Reaction Steps

A mixture of ethyl 1-benzyloxycarbonylpiperidine-4-oxyacetate (2.4 g) and 2-methoxyethylamine (5 ml) was heated on a steam bath for 6 hours. The amine was evaporated under reduced pressure and the residue was dissolved in ethyl acetate (10 ml), washed sequentially with dilute citric acid solution (5 ml), water (5 ml) and saturated aqueous sodium chloride (5 ml), dried (MgSO4) and concentrated. The residual oil was purified by flash column chromatography, eluting with hexane/ethyl acetate (1:3) to give N-2-methoxyethyl-1-benzyloxycarbonylpiperidine-4-oxyacetamide (500 mg) as a colourless oil. NMR: (d6DMSO): δ1.4-1.5(2H,m); 1.75-1.9(2H,m); 3.0-3.4(9H,m); 3.55(1H,m); 3.65-3.8(2H,m); 3.9(2H,s); 5.1(2H,s); 7.3(5H,m); 7.6(1H, br. t); m/e 351(M+H)+, 373 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563141
Source datasetuspto-grants-1996_10
ORD IDord-909f63792efc4760a0c0ee1184caa51c
Source noteuspto-grants-1996_10